56660
Hydrocinnamaldehyde
technical, ≥90% (GC)
Synonym(s):
3-Phenylpropionaldehyde
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About This Item
Linear Formula:
C6H5CH2CH2CHO
CAS Number:
Molecular Weight:
134.18
EC Number:
203-211-8
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1071910
MDL number:
grade
technical
assay
≥90% (GC)
refractive index
n20/D 1.523
bp
97-98 °C/12 mmHg (lit.)
density
1.019 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
[H]C(=O)CCc1ccccc1
InChI
1S/C9H10O/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6,8H,4,7H2
InChI key
YGCZTXZTJXYWCO-UHFFFAOYSA-N
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Samir BouzBouz et al.
Organic letters, 5(11), 1995-1997 (2003-05-24)
[reaction: see text] The synthesis of (+)-strictifolione was achieved from 3-phenylproprionaldehyde by using enantioselective allyltitanations to control the stereogenic centers at C6, C4', and C6' and a cross-methathesis to control the configuration of the double bond at C1'-C2'.
Takashi Ooi et al.
Journal of the American Chemical Society, 126(31), 9685-9694 (2004-08-05)
A highly efficient direct asymmetric aldol reaction of a glycinate Schiff base with aldehydes has been achieved under mild organic/aqueous biphasic conditions with excellent stereochemical control, using chiral quaternary ammonium salt 1b as a phase-transfer catalyst. The initially developed reaction
Shih-Shen Chou Lin et al.
Phytotherapy research : PTR, 25(10), 1511-1518 (2011-03-12)
The purpose of this study was to analyse the major compound in the leaf essential oil of Cinnamomum osmophloeum Kaneh. and to examine its in vivo toxicity and cytokine-modulatory effects. The HS-GC/MS and quantitative HPLC analyses showed the concentrations of
The arduous way to the egg: follow the nose.
Stefan Bartram et al.
Angewandte Chemie (International ed. in English), 42(39), 4729-4731 (2003-10-17)
G M Raner et al.
Journal of inorganic biochemistry, 81(3), 153-160 (2000-10-29)
The reaction of hydrogen peroxide and certain aromatic aldehydes with cytochrome P450BM3-F87G results in the covalent modification of the heme cofactor of this monooxygenase. Analysis of the resulting heme by electronic absorption spectrophotometry indicates that the reaction in the BM3
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